US3250834A - Method for making foamable polystrene pellets - Google Patents
Method for making foamable polystrene pellets Download PDFInfo
- Publication number
- US3250834A US3250834A US210910A US21091062A US3250834A US 3250834 A US3250834 A US 3250834A US 210910 A US210910 A US 210910A US 21091062 A US21091062 A US 21091062A US 3250834 A US3250834 A US 3250834A
- Authority
- US
- United States
- Prior art keywords
- strands
- rolls
- roll
- pellets
- foamable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 16
- 239000008188 pellet Substances 0.000 title description 9
- 238000001125 extrusion Methods 0.000 description 16
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 10
- -1 e.g. Polymers 0.000 description 10
- 229920005992 thermoplastic resin Polymers 0.000 description 10
- 239000002826 coolant Substances 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 239000004793 Polystyrene Substances 0.000 description 8
- 229920002223 polystyrene Polymers 0.000 description 8
- 229920001169 thermoplastic Polymers 0.000 description 7
- 239000004416 thermosoftening plastic Substances 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 230000002093 peripheral effect Effects 0.000 description 6
- 239000004088 foaming agent Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 239000012815 thermoplastic material Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
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- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
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- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
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- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
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- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
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- 238000007385 chemical modification Methods 0.000 description 1
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- 230000003750 conditioning effect Effects 0.000 description 1
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- JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
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- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
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- B29C44/34—Auxiliary operations
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- B29C44/46—Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
- B29C44/461—Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length dispensing apparatus, e.g. dispensing foaming resin over the whole width of the moving surface
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- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/20—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by expressing the material, e.g. through sieves and fragmenting the extruded length
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- B29B9/00—Making granules
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
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- B29C48/345—Extrusion nozzles comprising two or more adjacently arranged ports, for simultaneously extruding multiple strands, e.g. for pelletising
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- C08J9/16—Making expandable particles
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
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- B29C2948/92504—Controlled parameter
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- B29C2948/92819—Location or phase of control
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- B29C2948/92876—Feeding, melting, plasticising or pumping zones, e.g. the melt itself
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- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
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-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2025/00—Use of polymers of vinyl-aromatic compounds or derivatives thereof as moulding material
- B29K2025/04—Polymers of styrene
- B29K2025/06—PS, i.e. polystyrene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2101/00—Use of unspecified macromolecular compounds as moulding material
- B29K2101/12—Thermoplastic materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
Definitions
- This invention relates to a novel process for producing foamable thermoplastic material in strand, pellet, or granular form and, more particularly, relates to processes for making granular foamable thermoplastic material of high quality, eminently suitable for extrusion to form foamed articles.
- foamable thermoplastic particles have heretofore been known. However, such methods produced a foamable thermoplastic material which was unsuitable for extrusion into foamed articles without first conditioning said particles in one way or anotherto make them suitable for use in extrusion apparatus.
- one prior method for making foamable particles required the use of a liquid coolant in contact with the hot foamable particles to cool them below the foaming or expanding temperature. The use of liquid coolants invariably brought about certain physical and/ or chemical modifications to the particles, thus requiring additional treatments to make them suitable for use in the subsequent extrusion of foamed articles.
- a principal object of this invention is to provide a process for producing foamable thermoplastic pellets or particles which are eminently suited for use in subsequent extrusion procedures to form foamed articles.
- Another object is the provision of a process for producing foamable thermoplastic pellets or particles which can be subsequently extruded to form foamed articles without the necessity of special intermediate treatments.
- a further object is the provision of a process for producing foamable thermoplastic particles or pellets which process and apparatus are characterized by simplicity, efiiciency, and high rates of production.
- Another object is the provision of a process for forming foamable thermoplastic pellets or particles which have not been adversely chemically or physically modified by the use of liquid coolants and which can be directly extruded to form foamed articles without any special prior treatment.
- FIG. 1 is a diagrammatic side elevation of an embodiment of this invention
- FIG. 2 is a section taken on line 22 of FIG. 1;
- FIG. 3 is a section taken on line 3-3 of FIG. 1;
- FIG. 4 is a perspective view of a chilled roll which is partially cut away.
- FIG. 1 an extruder 1 having a hopper 2, an injection tube 3, and an extrusion die 4.
- the extruder can be of the conventional type and the extrusion die, as best shown in FIG. 3, is of the type employed for extruding strands.
- the extrusion die 4, as shown in the embodiment of the figures, comprises a plurality of orifices 5 and is tapered in the direction of extrusion such that the smallest cross-sectional area of said die is at the orifices 5 and the crosssection of said die progressively increases towards the extruder l with the distance from said orifices.
- a main chilled roll 6 is provided adjacent and slightly below the extrusion die 4 such'that the strands, as extruded from the orifices 5, are substantially tangential to said roll.
- a smaller chilled roll 7 is positioned above in 3,259,834. Patented May 10, 1966 "ice substantial tangential contact with the main chilled roll 6 such that strands being extruded from the orifices 5 are directed into the nip formedby the rolls 6 and 7.
- Secondary chilled rolls 8 are positioned in substantial contact with the main chilled roll along a substantial portion of the periphery thereof.
- Guide roll 9, which may or may not be chilled, is positioned in substantial contact with the main chilled roll 6 at a point after the points of contact of secondary chilled rolls 8 with said main chilled roll. All of the chilled rolls 6, 7 and 8 are provided with means for circulating a coolant therethrough.
- coolant may be of any suitable type, chilled water probably being the most expedient coolant.
- the tapered forward end of the extrusion die 4 extends into the nip formed by the rolls 6 and 7 preferably without contacting either of said rolls.
- the distance the strands S must travel after leaving the orifices 5 and before contacting the roll 6 or 7 should be short, e.g., two inches, or less.
- Additional guide rolls 10 are provided to suitably guide the strands S as they come off of guide roll 9. All of the rolls 6, 7, and 8 are provided with aligned endless grooves 11 in the peripheral surfaces thereof, as best shown in FIG. 2 with relation to rolls 6 and 7.
- the cross-sectional shape of the grooves 11 is not narrowly critical and, instead of being triangular as shown in FIG. 2, the cross-section can be semi-circular or of any other suitable shape.
- the size of the grooves 11 is somewhat more critical than the shape andshould be large enough to accommodate the strands S without unduly deforming said strands but should be small enough to provide an adequate cooling contact surface to said strands. It has been found that the triangular cross-section of the grooves 11 provides an excellent cooling contact surface for the strands S Without unduly deforming said strands.
- Suitable driving means of any conventional type is employed to drive the rolls 6, 7, 8, 9, and 10 in the respective directions required to move the strand S from the extrusion die past the last guide roll 10. The directions of rotation of each of said rolls are shown in FIG. 1.
- nozzles 12 are disposed between the rolls 7 and 8 and adjacent rolls 8.
- the nozzles 12 are directed towards the strands S disposed in the grooves 11 onmain chilled roll 6.
- the nozzles 12 are connected through conduits 13 to a supply of cool air 14.
- the supply 14, in its most simple form, is a suction fan pulling cool air in and forcing it through conduits 13. It is not critically necessary to specially cool the air distributed to the nozzles 12, although such an expediency can be employed.
- Adjacent the last guide roll 10 is positioned a pelletizer or cutter 15 which receives the strands S from said last guide roll and cuts said strands into granular form.
- foamable thermoplastic strands S are extruded from the orifices 5 into the nip of rolls 6 and 7.
- the strands S are received in the grooves 11 which are aligned with the orifices 5 and travel around a major portion of the periphery of the main chilled roll 6, thereby cooling said strands below the expanding temperature of said strands at atmospheric pressure.
- the secondary chilled rolls 7 and 8 assist in cooling the strands as does the air ejected from the nozzles 12.
- the strands then are guided by guide rolls 9 and 10 into the pelletizer 15 where they are cut into granular form.
- a heat-plasticized, homogeneous, intimately admixed mixture of polystyrene and 4 percent of pentane is supplied to the extrusion die 4 and is extruded at a tempera- 3 ture of about 250 F. through the orifices 5 to form strands S.
- the strands S are introduced into the nip of rolls 6 and 7 in such a manner that a strand is disposed in a groove 11 in the peripheral surfaces of said rolls 6 and 7.
- the main roll 6 is maintained at a temperature of 45 F. and the strands being extruded have an approximate diameter of 0.06 inch.
- the rolls 6 and 7 are driven in the respective directions shown in FIG. 1 to advance the strands S away from the extrusion die 4.
- the length of travel of the strands on the main roll 6 is approximately 24 inches and the production of strands is about 200 pounds per hour.
- the strands After the strands have traveled in the grooves 11 of the main roll 6 for a sufiicient distance (approximately 24 inches), to cool them to a temperature below the heat distortion temperature of the polystyrenepentane material composing said strands, they are passed around guide roll 9 and guided by guide rolls 10 into the pelletizer 15. Normal room temperature air (at about 75 F.) is circulated through the cooling system 14 and ejected from the nozzles 12 onto the strands as they pass over the main roll 6.
- the secondary rolls 7 and 8 are also cooled to a temperature of approximately 45 F.
- the temperature at which the thermoplastic mixture is extruded from the orifices 5 is not narrowly critical and can range from 225 F. to 375 F.
- the pressure within the extrusion die 4, when extruding at 225 F., should be approximately 500 p.s.i. and can run as high as 4,000 p.s.i. when extruding at high temperatures.
- the temperature of the rolls 6, 7 and 8 also is not narrowly critical and can range from F. to 100 F.
- the primary function of the secondary rolls 7 and 8 is to maintain the strands in close contact with the main roll 6 and, additionally, when said secondary rolls 7 and 8 are cooled, they assist in cooling the strands. It is quite important that no liquid coolant be brought into contact with the hot strands.
- the main roll -6 can be any endless, rigid, arcuate to flat surface.
- a cooled conveyor belt having endless grooves therein can be passed in front of the orifices to receive and cool the strands being extruded therefrom.
- the secondary rolls 7 and 8 can be employed with the conveyor belt or can be in the form of conveyor belts themselves.
- the surfaces of each of the rolls or conveyor belts 6, 7 and 8 which contact the strands are made of heat-conductive material so as to remove heat from said strands and transfer it to a cooling medium.
- polystyrene in pellet or granular form is added into hopper 2.
- the polystyrene is then heat-plasticized at a suitable temperature, e.g., 350 F. to 450 F., and is somewhat decompressed as it approaches the injection tube 3.
- the pentane is introduced into the polystyrene through injection tube 3 and the resulting mixture enters a mixing and coolingzone at a suitable temperature of about 200 F. to 300 F. Thereafter, the resulting mixture is extruded at a suitable temperature, preferably below 325 F.
- interpolymers of the above mentionedvinylidene monomers with unsaturated alpha,beta-unsaturated polycarboxylic acids and derivatives thereof e.g., maleic anhydride, diethyl maleate, dibutyl fumarate, diallyl maleate, dipropyl maleate, etc.
- thermoplastic resins such as homopolymers and interpolymers of vinyl chloride, homopolymers of vinylidene aromatic hydrocarbon compounds and ring halogenated derivatives thereof, e.g., styrene, o-chlorostyrene, 'p-chlorostyrene, 2,5-dichlorostyrene, 2,4-dichlorostyrene, p-meth'ylstyrene, p-ethylstyrene, vinyl naphthalene, alpha-methylstyrene, and interpolymers of such vinylidene aromatic hydrocarbon compounds with other vinylidene monomers in which the interpolymer contains at least 70% of the vinylidene aromatic hydrocarbon compounds.
- thermoplastic resins such as a blend of styrene and a rubbery polymer, e.g., natural rubber, butadieneacrylonitrile rubbers and the like.
- a rubbery polymer e.g., natural rubber, butadieneacrylonitrile rubbers and the like.
- High impact polystyrene prepared by polymerizing monomeric styrene in the presence of a rubbery diene polymer also may be employed advantageously.
- Suitable foaming agents for the thermoplastic resins are Well known and the selection of the particular foaming agents to be employed will be dictated largely by the particular thermoplastic resin in which it is to be incorporated. It is preferred to employ as foaming agents nonreactive organic liquids which have not more than a slight solvent action on the thermoplastic resin and which volatilize below the softening point of the thermoplastic resin. Such agents include these boiling between F. to 200 F.
- foaming agents examples include pentane, hexane, heptane, petroleum ether, cyclopentane, cyclopentadiene, acetone, methanol, methyl acetate, ethyl acetate, methyl formate, ethyl formate, dichloroethylene, isopropyl chloride, propionalde'hyde, and diisopropyl ether.
- foaming agent will be employed in the amount of about 2 /2l0 and preferably 5-8 weight percent of the thermoplastic resin.
- pansion is obtained'ble by pressure contacting the strands of foamable thermoplastic material between the main roll 6 and any one or more of auxiliary rolls 7 through 9. This is accomplished by making the grooves 11 of a size smaller than the strand S as it reaches the rolls, such that the surfaces of said grooves pressure-contact the surfaces of said strands.
- a process for making a foamable polystyrene composition which contains pentane in addition to polystyrene uniformly dispersed throughout without contacting said foamable composition with a liquid coolant such as water, said process comprising the steps of, supplying a uniform, heat-plasticized mass comprised of said polystyrene and pentane to a plurality of extrusion orifices arranged side by side at a temperature of about 225 F. to 375 F.
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Description
F. H. COLLINS May 10, 1966 METHOD FOR MAKING FOAMABLE POLYS'IYRENE PELLETS Filed July 19, 1962 R fl no; m M New. m M f w w N\ w ATTORNEYS United States Patent This invention relates to a novel process for producing foamable thermoplastic material in strand, pellet, or granular form and, more particularly, relates to processes for making granular foamable thermoplastic material of high quality, eminently suitable for extrusion to form foamed articles.
Methods for making foamable thermoplastic particles have heretofore been known. However, such methods produced a foamable thermoplastic material which was unsuitable for extrusion into foamed articles without first conditioning said particles in one way or anotherto make them suitable for use in extrusion apparatus. For example, one prior method for making foamable particles required the use of a liquid coolant in contact with the hot foamable particles to cool them below the foaming or expanding temperature. The use of liquid coolants invariably brought about certain physical and/ or chemical modifications to the particles, thus requiring additional treatments to make them suitable for use in the subsequent extrusion of foamed articles.
A principal object of this invention is to provide a process for producing foamable thermoplastic pellets or particles which are eminently suited for use in subsequent extrusion procedures to form foamed articles.
Another object is the provision of a process for producing foamable thermoplastic pellets or particles which can be subsequently extruded to form foamed articles without the necessity of special intermediate treatments.
A further object is the provision of a process for producing foamable thermoplastic particles or pellets which process and apparatus are characterized by simplicity, efiiciency, and high rates of production.
Another object is the provision of a process for forming foamable thermoplastic pellets or particles which have not been adversely chemically or physically modified by the use of liquid coolants and which can be directly extruded to form foamed articles without any special prior treatment.
Further objects and advantages of this invention are apparent from the following description taken in conjunction with the appended drawings, in which:
FIG. 1 is a diagrammatic side elevation of an embodiment of this invention;
FIG. 2 is a section taken on line 22 of FIG. 1;
FIG. 3 is a section taken on line 3-3 of FIG. 1; and
FIG. 4 is a perspective view of a chilled roll which is partially cut away.
Referring now to the figures, there is shown in FIG. 1 an extruder 1 having a hopper 2, an injection tube 3, and an extrusion die 4. The extruder can be of the conventional type and the extrusion die, as best shown in FIG. 3, is of the type employed for extruding strands. The extrusion die 4, as shown in the embodiment of the figures, comprises a plurality of orifices 5 and is tapered in the direction of extrusion such that the smallest cross-sectional area of said die is at the orifices 5 and the crosssection of said die progressively increases towards the extruder l with the distance from said orifices.
A main chilled roll 6 is provided adjacent and slightly below the extrusion die 4 such'that the strands, as extruded from the orifices 5, are substantially tangential to said roll. A smaller chilled roll 7 is positioned above in 3,259,834. Patented May 10, 1966 "ice substantial tangential contact with the main chilled roll 6 such that strands being extruded from the orifices 5 are directed into the nip formedby the rolls 6 and 7. Secondary chilled rolls 8 are positioned in substantial contact with the main chilled roll along a substantial portion of the periphery thereof. Guide roll 9, which may or may not be chilled, is positioned in substantial contact with the main chilled roll 6 at a point after the points of contact of secondary chilled rolls 8 with said main chilled roll. All of the chilled rolls 6, 7 and 8 are provided with means for circulating a coolant therethrough. The
coolant may be of any suitable type, chilled water probably being the most expedient coolant. It is to be noted that the tapered forward end of the extrusion die 4 extends into the nip formed by the rolls 6 and 7 preferably without contacting either of said rolls. The distance the strands S must travel after leaving the orifices 5 and before contacting the roll 6 or 7 should be short, e.g., two inches, or less. Additional guide rolls 10 are provided to suitably guide the strands S as they come off of guide roll 9. All of the rolls 6, 7, and 8 are provided with aligned endless grooves 11 in the peripheral surfaces thereof, as best shown in FIG. 2 with relation to rolls 6 and 7. The cross-sectional shape of the grooves 11 is not narrowly critical and, instead of being triangular as shown in FIG. 2, the cross-section can be semi-circular or of any other suitable shape. The size of the grooves 11 is somewhat more critical than the shape andshould be large enough to accommodate the strands S without unduly deforming said strands but should be small enough to provide an adequate cooling contact surface to said strands. It has been found that the triangular cross-section of the grooves 11 provides an excellent cooling contact surface for the strands S Without unduly deforming said strands. Suitable driving means of any conventional type is employed to drive the rolls 6, 7, 8, 9, and 10 in the respective directions required to move the strand S from the extrusion die past the last guide roll 10. The directions of rotation of each of said rolls are shown in FIG. 1.
As an auxiliary cooling system, nozzles 12 are disposed between the rolls 7 and 8 and adjacent rolls 8. The nozzles 12 are directed towards the strands S disposed in the grooves 11 onmain chilled roll 6. The nozzles 12 are connected through conduits 13 to a supply of cool air 14. The supply 14, in its most simple form, is a suction fan pulling cool air in and forcing it through conduits 13. It is not critically necessary to specially cool the air distributed to the nozzles 12, although such an expediency can be employed.
Adjacent the last guide roll 10 is positioned a pelletizer or cutter 15 which receives the strands S from said last guide roll and cuts said strands into granular form.
In operation, foamable thermoplastic strands S are extruded from the orifices 5 into the nip of rolls 6 and 7. The strands S are received in the grooves 11 which are aligned with the orifices 5 and travel around a major portion of the periphery of the main chilled roll 6, thereby cooling said strands below the expanding temperature of said strands at atmospheric pressure. The secondary chilled rolls 7 and 8 assist in cooling the strands as does the air ejected from the nozzles 12. The strands then are guided by guide rolls 9 and 10 into the pelletizer 15 where they are cut into granular form.
The following example is presented. All percentages are based on the weight of polystyrene.
Example. 7
A heat-plasticized, homogeneous, intimately admixed mixture of polystyrene and 4 percent of pentane is supplied to the extrusion die 4 and is extruded at a tempera- 3 ture of about 250 F. through the orifices 5 to form strands S. The strands S are introduced into the nip of rolls 6 and 7 in such a manner that a strand is disposed in a groove 11 in the peripheral surfaces of said rolls 6 and 7. The main roll 6 is maintained at a temperature of 45 F. and the strands being extruded have an approximate diameter of 0.06 inch. The rolls 6 and 7 are driven in the respective directions shown in FIG. 1 to advance the strands S away from the extrusion die 4. The length of travel of the strands on the main roll 6 is approximately 24 inches and the production of strands is about 200 pounds per hour. After the strands have traveled in the grooves 11 of the main roll 6 for a sufiicient distance (approximately 24 inches), to cool them to a temperature below the heat distortion temperature of the polystyrenepentane material composing said strands, they are passed around guide roll 9 and guided by guide rolls 10 into the pelletizer 15. Normal room temperature air (at about 75 F.) is circulated through the cooling system 14 and ejected from the nozzles 12 onto the strands as they pass over the main roll 6. The secondary rolls 7 and 8 are also cooled to a temperature of approximately 45 F.
The temperature at which the thermoplastic mixture is extruded from the orifices 5 is not narrowly critical and can range from 225 F. to 375 F. The pressure within the extrusion die 4, when extruding at 225 F., should be approximately 500 p.s.i. and can run as high as 4,000 p.s.i. when extruding at high temperatures. The temperature of the rolls 6, 7 and 8 also is not narrowly critical and can range from F. to 100 F. The primary function of the secondary rolls 7 and 8 is to maintain the strands in close contact with the main roll 6 and, additionally, when said secondary rolls 7 and 8 are cooled, they assist in cooling the strands. It is quite important that no liquid coolant be brought into contact with the hot strands.
The main roll -6 can be any endless, rigid, arcuate to flat surface. For example, instead of being in the form of a roll, a cooled conveyor belt having endless grooves therein can be passed in front of the orifices to receive and cool the strands being extruded therefrom. Similarly, the secondary rolls 7 and 8 can be employed with the conveyor belt or can be in the form of conveyor belts themselves. The surfaces of each of the rolls or conveyor belts 6, 7 and 8 which contact the strands are made of heat-conductive material so as to remove heat from said strands and transfer it to a cooling medium.
In forming the heat-plasticized mixture in the extruder 1, polystyrene in pellet or granular form is added into hopper 2. The polystyrene is then heat-plasticized at a suitable temperature, e.g., 350 F. to 450 F., and is somewhat decompressed as it approaches the injection tube 3. The pentane is introduced into the polystyrene through injection tube 3 and the resulting mixture enters a mixing and coolingzone at a suitable temperature of about 200 F. to 300 F. Thereafter, the resulting mixture is extruded at a suitable temperature, preferably below 325 F.
The foamable thermoplastic resin compositions which can be extruded by the method and apparatus of this invention consists of a thermoplastic resin and a suitable foaming or pore-forming agent. Examples of thermoplastic resins that may be employed include cellulose ethers and esters, e.g., ethyl cellulose, cellulose acetate; homopolymers and interpolymers of monomeric compounds containing the CH =C grouping such as olefins, e.g., ethylene, isobutylene; vinyl halides, e.g., vinyl chloride; vinylidene chloride; vinyl esters of carboxylic acids, e.g., vinyl acetate, vinyl butyrate, vinyl stearate, vinyl benzoate; vinyl ethers, e.g., vinyl methyl ether, vinyl ethyl ether, vinyl isobutyl ether; unsaturated carboxylic acids and derivatives thereof, e.g., acrylic' acid, methacrylic acid, methyl acrylate, ethyl acrylate, methyl methacrylate, acrylarnide, acrylonitrile, methacrylonitrile, and
interpolymers of the above mentionedvinylidene monomers with unsaturated alpha,beta-unsaturated polycarboxylic acids and derivatives thereof, e.g., maleic anhydride, diethyl maleate, dibutyl fumarate, diallyl maleate, dipropyl maleate, etc. In general, optimum results are obtained with rigid, relatively non-elastic thermoplastic resins such as homopolymers and interpolymers of vinyl chloride, homopolymers of vinylidene aromatic hydrocarbon compounds and ring halogenated derivatives thereof, e.g., styrene, o-chlorostyrene, 'p-chlorostyrene, 2,5-dichlorostyrene, 2,4-dichlorostyrene, p-meth'ylstyrene, p-ethylstyrene, vinyl naphthalene, alpha-methylstyrene, and interpolymers of such vinylidene aromatic hydrocarbon compounds with other vinylidene monomers in which the interpolymer contains at least 70% of the vinylidene aromatic hydrocarbon compounds. It is feasible and sometimes desirable to employ a blend of two or more thermoplastic resins such as a blend of styrene and a rubbery polymer, e.g., natural rubber, butadieneacrylonitrile rubbers and the like. High impact polystyrene prepared by polymerizing monomeric styrene in the presence of a rubbery diene polymer also may be employed advantageously.
Suitable foaming agents for the thermoplastic resins are Well known and the selection of the particular foaming agents to be employed will be dictated largely by the particular thermoplastic resin in which it is to be incorporated. It is preferred to employ as foaming agents nonreactive organic liquids which have not more than a slight solvent action on the thermoplastic resin and which volatilize below the softening point of the thermoplastic resin. Such agents include these boiling between F. to 200 F. Examples of suitable foaming agents that may be employed'include pentane, hexane, heptane, petroleum ether, cyclopentane, cyclopentadiene, acetone, methanol, methyl acetate, ethyl acetate, methyl formate, ethyl formate, dichloroethylene, isopropyl chloride, propionalde'hyde, and diisopropyl ether. Usually the foaming agent will be employed in the amount of about 2 /2l0 and preferably 5-8 weight percent of the thermoplastic resin.
Important advantages in pansion are obtain'ble by pressure contacting the strands of foamable thermoplastic material between the main roll 6 and any one or more of auxiliary rolls 7 through 9. This is accomplished by making the grooves 11 of a size smaller than the strand S as it reaches the rolls, such that the surfaces of said grooves pressure-contact the surfaces of said strands.
The above description and particularly the example are set forth by way of illustration only. It will be obvious to those skilled in the art that many variations and modification thereof can be made without departing from the spirit and scope of the invention herein described.
What is claimed is:
A process for making a foamable polystyrene composition which contains pentane in addition to polystyrene uniformly dispersed throughout without contacting said foamable composition with a liquid coolant such as water, said process comprising the steps of, supplying a uniform, heat-plasticized mass comprised of said polystyrene and pentane to a plurality of extrusion orifices arranged side by side at a temperature of about 225 F. to 375 F. and at a pressure to prevent expansion, extruding said mass through said orifices in the form of a plurality of strands into a zone of substantially atmospheric pressure, and substantially immediately, and prior to appreciable expansion of the extruded material disposing each of said strands in a groove formed in the peripheral surface of a large rotating roll and at about the same time in a groove formed in the peripheral surface of a first small rotating roll mating with said large rotating roll to enclose said strands between said large roll and small roll, thereafter retaining each of said strands in said groove of said large roll while successively disposing each of said strands in cooling and prevention of exgrooves formed in the peripheral surfaces of successive small rolls mating with said large roll around the peripheral surface thereof, all of said rolls being maintained at a temperature below the expanding temperature of said extruded material at atmospheric pressure to cool said extruded material to a temperature below the expanding temperature thereof at atmospheric pressure, directing cooling air on said strands immediately as they exit from said orifices, and thereafter removing said strands from said grooves and cutting said strands into pellets.
References Cited by the Examiner UNITED STATES PATENTS 345,539 7/1886 Pfanukuchi. 2,289,774 '7/ 1942 Graves. 2,294,630 9/ 1942 Reichel et al. 2,374,069 4/1945 Balthis. 2,401,236 5/ 1946 Fielitz. 2,582,294 1/ 1952 Stober.
6 Roggi et a1. Carlson. Rubens et a1. Engles. Latferty. Root. Washbu'rn. Daester.
FOREIGN PATENTS Great Britain.- Canada. Italy.
15 ROBERT F. WHITE, Primary Examiner.
MORRIS LIEBMAN, Examiner.
P. E. ANDERSON, S. A. HELLER,
Assistant Examiners.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US210910A US3250834A (en) | 1962-07-19 | 1962-07-19 | Method for making foamable polystrene pellets |
| GB34541/62A GB1005901A (en) | 1962-07-19 | 1962-09-10 | Process for making a foamable polymeric composition in pellet form |
| DE19641504854 DE1504854A1 (en) | 1962-07-19 | 1964-04-17 | Method and device for producing tablets |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US210910A US3250834A (en) | 1962-07-19 | 1962-07-19 | Method for making foamable polystrene pellets |
| DES0090602 | 1964-04-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3250834A true US3250834A (en) | 1966-05-10 |
Family
ID=25997628
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US210910A Expired - Lifetime US3250834A (en) | 1962-07-19 | 1962-07-19 | Method for making foamable polystrene pellets |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3250834A (en) |
| DE (1) | DE1504854A1 (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3767344A (en) * | 1970-09-15 | 1973-10-23 | Riwisa Ag Kunststoffwerke Hagg | Apparatus for reprocessing plastic scrap material |
| US3900544A (en) * | 1973-11-28 | 1975-08-19 | Arco Polymers Inc | Method for the continuous extrusion of multiple small cross-section thermoplastic polymeric resinous foam profiles |
| US4107250A (en) * | 1974-11-08 | 1978-08-15 | Standard Oil Company (Indiana) | Process for making fiber-reinforced thermoplastic pellets |
| US4194872A (en) * | 1976-09-04 | 1980-03-25 | Reifenhauser Kg | Apparatus for the cooling, calibrating and straightening of a plate-shaped continuously extruded synthetic-resin strand |
| US4336010A (en) * | 1980-09-02 | 1982-06-22 | Thompson Daniel T | Dough forming, dividing and cutting apparatus |
| US4340342A (en) * | 1981-01-16 | 1982-07-20 | The B. F. Goodrich Company | Apparatus for processing elastomeric materials |
| US4413965A (en) * | 1981-05-08 | 1983-11-08 | Nihon Repromachine Kogyo Kabushiki Kaisha | Pelletizing device for plastic material |
| US4749535A (en) * | 1985-04-05 | 1988-06-07 | Yasuo Matsuda | Method and apparatus for forming profiled plastic products involving extrusion, roller shaping and cutting |
| US5064869A (en) * | 1989-12-27 | 1991-11-12 | General Electric Company | Polyphenlene ether foams from low i.v. polyphenylene ether expandable microparticles |
| US5091256A (en) * | 1989-12-27 | 1992-02-25 | General Electric Company | Polyphenylene ether foams from low I.V. polyphenylene ether expandable microparticles |
| US5095041A (en) * | 1989-12-27 | 1992-03-10 | General Electric Company | Simple process for imbibing blowing agents in thermoplastic resin granules |
| US5130340A (en) * | 1990-07-09 | 1992-07-14 | General Electric Company | Elastomeric low density foamable compositions and process of making the same and articles made therefrom |
| US5190986A (en) * | 1990-07-09 | 1993-03-02 | General Electric Company | Elastomeric low density foamable compositions and process of making the same and articles made therefrom |
| US5310515A (en) * | 1991-10-08 | 1994-05-10 | Reiter Automatik Apparate-Maschinebau Gmbh | Process to cool and pelletize molten strands issuing from nozzles |
| US6039905A (en) * | 1994-11-07 | 2000-03-21 | C.F.Scheer & Cie Gmbh & Co. | Apparatus and method for granulating plastic strands |
| US20120061867A1 (en) * | 2010-09-10 | 2012-03-15 | Playtex Products Llc | Polymer pellets containing supercritical fluid and methods of making and using |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108602203A (en) * | 2016-02-29 | 2018-09-28 | 株式会社理光 | Strand manufacturing equipment and strand manufacturing method |
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| US4749535A (en) * | 1985-04-05 | 1988-06-07 | Yasuo Matsuda | Method and apparatus for forming profiled plastic products involving extrusion, roller shaping and cutting |
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| US5095041A (en) * | 1989-12-27 | 1992-03-10 | General Electric Company | Simple process for imbibing blowing agents in thermoplastic resin granules |
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| US5190986A (en) * | 1990-07-09 | 1993-03-02 | General Electric Company | Elastomeric low density foamable compositions and process of making the same and articles made therefrom |
| US5310515A (en) * | 1991-10-08 | 1994-05-10 | Reiter Automatik Apparate-Maschinebau Gmbh | Process to cool and pelletize molten strands issuing from nozzles |
| US6039905A (en) * | 1994-11-07 | 2000-03-21 | C.F.Scheer & Cie Gmbh & Co. | Apparatus and method for granulating plastic strands |
| US20120061867A1 (en) * | 2010-09-10 | 2012-03-15 | Playtex Products Llc | Polymer pellets containing supercritical fluid and methods of making and using |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1504854A1 (en) | 1969-09-25 |
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